RICO Hand Sanitizer Wipes

Manufacturer
HANUL CO.,LTD
Effective date
2025-01-20
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 00:53:16

Label at a glance#

ProductRICO Hand Sanitizer Wipes
Active ingredientALCOHOL
Label structure11 sections

Dosage and administration

Adults and children 2 years and over apply to hands Wet hands thoroughly with product and allow to dry Children under 2 years ask doctor before use Not recommended for infants

Storage and handling

do not store above 105ºF/40°C may discolor some fabrics harmful to wood finishes and plastics

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 80% Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer Wipes

Use

INDICATIONS & USAGE SECTION

To decrease bacteria on the skin that could cause disease

Warnings

WARNINGS SECTION

For external use only: hands

Flammable. Keep away from fire and flame.

OTC - WHEN USING SECTION

When using this product

keep out of eyes. In case of contact with eyes, flush thoroughly with water.

avoid contact with broken skin

do not inhale or ingest

OTC - STOP USE SECTION

Stop Use and ask a doctor if

irritation or redness develops

condition persists for more than 72 hours

These may be signs of a serious condition

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Adults and children 2 years and over
  • apply to hands
  • Wet hands thoroughly with product and allow to dry
  • Children under 2 years ask doctor before use
  • Not recommended for infants

Other information

STORAGE AND HANDLING SECTION

do not store above 105ºF/40°C

may discolor some fabrics

harmful to wood finishes and plastics

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf Extract, Butylene Glycol, Citric Acid, Purified water USP, glycerin, hydrogen peroxide,1,2 Hexanediol,

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11NDC: 75214-900-01

RICO HAND SANITIZING WIPES 80 % ALCOHOL + HYDROGEN PEROXIDE

[“Reducing bacteria and viruses such as Salmonella, Staphylococcus aureus and SARS-CoV-2 Delta variant that causes COVID-19”

NON STERILE SOLUTION

100 wipes

wipes dimension 6in. x 8 In (15cm x 20m)

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2361646ethanol 80 % Medicated PadPSN3
2361646ethanol 0.8 ML/ML Medicated PadSCD3
2361646ethanol 80 % Medicated WipesSY3
2361646ethyl alcohol 80 % Topical ClothSY3

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75214-900-01RICO Hand Sanitizer Wipes834 mL in 1 PACKAGECLOTH8343

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75214-900RICO HAND SANITIZER WIPES (ALCOHOL) CLOTH [HANUL CO.,LTD]3Current NDC, Legacy NDC, 1 package rows20250121_dc8ba3a2-9748-ec52-e053-2995a90a638b.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75214-90075214-900-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
RICO Hand Sanitizer WipesALCOHOLHANUL CO.,LTDdc8ba3a2-9748-ec52-e053-2995a90a638b2025-01-20WarningsExact identifier
ndc (package): 75214-900-01
ndc (product): 75214-900
ndc11 (package): 75214090001
spl id: 2c28f93c-99a1-f643-e063-6394a90a6f9d
spl set id: dc8ba3a2-9748-ec52-e053-2995a90a638b

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.